The Life Cycle Approach to Cleaning Validation 2018

Topics

• The FDA perspectives on cleaning validation and areas of concern during regulatory inspections
• The importance and underlying principles of cleaning validation and the requirements to have adequate cleaning procedures for manufacturing equipment in contact with the product
• Prepare and defend your own cleaning validation approach/program and avoid costly delays and/or rejections by regulatory agencies
• Cleaning validation procedures, protocols and reports that meet current FDA, WHO, PIC/S and EU regulations

Who should Attend

• Quality professionals
• Senior quality managers
• Validation engineers
• Production supervisors
• Quality engineers
• Process owners
• Quality auditors